{"id":13478,"date":"2016-03-24T10:21:58","date_gmt":"2016-03-24T01:21:58","guid":{"rendered":"http:\/\/mus.brc.riken.jp\/ja\/?page_id=13478"},"modified":"2021-04-07T14:08:55","modified_gmt":"2021-04-07T05:08:55","slug":"mar_2016_mm","status":"publish","type":"page","link":"http:\/\/mus.brc.riken.jp\/ja\/mouse_of_month\/mar_2016_mm","title":{"rendered":"March 2016 A knock-in mouse strain with R124H human TGFBI mutation"},"content":{"rendered":"<p><a href=\"\/ja\/mouse_of_month#2016\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-14572\" alt=\"Title201603\" src=\"\/ja\/wp-content\/uploads\/2016\/03\/Title201603.png\" width=\"502\" height=\"79\" \/><\/a><\/p>\n<table width=\"700\">\n<tbody>\n<tr>\n<td style=\"background-color: #ffffff; border: 0px; text-align: center;\">\n<p align=\"center\"><span style=\"font-size: x-large; line-height: 130%;\"><b>A knock-in mouse strain with R124H human TGFBI mutation<\/b><\/span><\/p>\n<h5><a href=\"https:\/\/brc.riken.jp\/mus\/RBRC09538\">B6-<i>Tgfbi&lt;tm1(TGFBI)Ccbko&gt;<\/i>\u00a0 (RBRC09538)<\/a><\/h5>\n<p><a href=\"\/ja\/wp-content\/uploads\/2016\/03\/201603.png\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone  wp-image-14575\" alt=\"201503\" src=\"\/ja\/wp-content\/uploads\/2016\/03\/201603.png\" width=\"754\" height=\"367\" \/><\/a><\/p>\n<p style=\"text-align: right;\" align=\"left\">Courtesy of Shigeto Shimmura, M.D., Ph.D.<\/p>\n<p align=\"left\">Granular and lattice deposits without edema and neovascularization were observed in the center of the cornea (A).<br \/>\nMasson trichrome and Congo red staining showed red deposits in the anterior cornea (B, C arrowhead).<\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>&nbsp;<\/p>\n<table width=\"700\">\n<tbody>\n<tr>\n<td style=\"border: 5px; background-color: #ffffff; text-align: left; white-space: normal; text-indent: 1em;\" valign=\"top\">\n<p align=\"left\">Granular corneal dystrophy (GCD) is an autosomal, bilateral disorder characterized by accumulation of granular deposits in the cornea. Age-dependent accumulation of these deposits affects central corneal stroma and decreases vision. Patients with GCD type 2 (GCD2, also known as Avellino type) tend to have less numerous deposits and may superficially resemble lattice corneal dystrophy. GCD2 is caused by a point mutation (R124H) in the <i>TGFBI<\/i> gene, which is the mutation most commonly found in Japanese patients [1, 2]. Shimmura and colleagues generated a knock-in mouse strain that carries human <i>TGFBI<\/i> cDNA with R124H mutation [3]. TGFBI<sup>R124H<\/sup> mice developed corneal opacities without inflammatory phenotype, and both granular opacities and lattice-like deposits were observed. Although the penetrance was not complete, the incidence of corneal opacity was significantly higher in homozygotes than in heterozygotes. While the phenotypes didn\u2019t become more severe in homozygous TGFBI<sup>R124H<\/sup> mice compared to those in heterozygotes, which is not the case in human, studies with this new GCD2 mouse model will contribute to reveal the pathogenesis of the disease.<\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>&nbsp;<\/p>\n<table width=\"700\">\n<tbody>\n<tr>\n<td style=\"border: 0px; background-color: #ffffff; text-align: right; white-space: nowrap;\" valign=\"top\">Depositor<\/td>\n<td style=\"border: 0px; background-color: #ffffff; text-align: center; white-space: nowrap;\" valign=\"top\">:<\/td>\n<td style=\"border: 0px; background-color: #ffffff; text-align: left; font-weight: bold;\" colspan=\"2\" valign=\"top\">Shigeto Shimmura, M.D., Ph.D.<br \/>\nDepartment of Ophthalmology<br \/>\nKeio University School of Medicine<\/td>\n<\/tr>\n<tr>\n<td style=\"border: 0px; background-color: #ffffff; text-align: right; white-space: nowrap;\" valign=\"top\">Strain name<\/td>\n<td style=\"border: 0px; background-color: #ffffff; text-align: center; white-space: nowrap;\" valign=\"top\">:<\/td>\n<td style=\"border: 0px; background-color: #ffffff; text-align: left; font-weight: bold;\" colspan=\"2\" valign=\"top\">B6-<i>Tgfbi&lt;tm1(TGFBI)Ccbko&gt;<\/i><\/td>\n<\/tr>\n<tr>\n<td style=\"border: 0px; background-color: #ffffff; text-align: right; white-space: nowrap;\" valign=\"top\">RBRC No.<\/td>\n<td style=\"border: 0px; background-color: #ffffff; text-align: center; white-space: nowrap;\" valign=\"top\">:<\/td>\n<td style=\"border: 0px; background-color: #ffffff; text-align: left;\" colspan=\"2\" valign=\"top\">RBRC09538<\/td>\n<\/tr>\n<tr>\n<td style=\"border: 0px; background-color: #ffffff; text-align: right; white-space: nowrap;\" rowspan=\"7\" valign=\"top\">References<\/td>\n<td style=\"border: 0px; background-color: #ffffff; text-align: center; white-space: nowrap;\" rowspan=\"7\" valign=\"top\">:<\/td>\n<td style=\"border: 0px; background-color: #ffffff; text-align: left;\" valign=\"top\">[1]<\/td>\n<td style=\"border: 0px; background-color: #ffffff; text-align: left;\" valign=\"top\">Folberg R, Alfonso E, Croxatto JO, Driezen NG, Panjwani N, Laibson PR, Boruchoff SA, Baum J, Malbran ES, Fernandez-Meijide R, et al. Clinically atypical granular corneal dystrophy with pathologic features of lattice-like amyloid deposits. A study of these families.<a href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/3278259\" target=\"_blank\" rel=\"noopener noreferrer\"><em>Ophthalmology<\/em>; 95(1):46-51, 1988.<\/a><\/td>\n<\/tr>\n<tr>\n<td style=\"border: 0px; background-color: #ffffff; text-align: left;\" valign=\"top\">[2]<\/td>\n<td style=\"border: 0px; background-color: #ffffff; text-align: left;\" valign=\"top\">Mashima Y, Yamamoto S, Inoue Y, Yamada M, Konishi M, Watanabe H, Maeda N, Shimomura Y, Kinoshita S. Association of autosomal dominantly inherited corneal dystrophies with BIGH3 gene mutations in Japan.<a href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/11024425\" target=\"_blank\" rel=\"noopener noreferrer\"><em>Am J Ophthalmol.<\/em>; 130(4):516-7, 2000.<\/a><\/td>\n<\/tr>\n<tr>\n<td style=\"border: 0px; background-color: #ffffff; text-align: left;\" valign=\"top\">[3]<\/td>\n<td style=\"border: 0px; background-color: #ffffff; text-align: left;\" valign=\"top\">Yamazoe K, Yoshida S, Yasuda M, Hatou S, Inagaki E, Ogawa Y, Tsubota K, Shimmura S. Development of a Transgenic Mouse with R124H Human TGFBI Mutation Associated with Granular Corneal Dystrophy Type 2.<a href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/26197481\" target=\"_blank\" rel=\"noopener noreferrer\"><em>PLoS ONE<\/em>; 10(7):e0133397, 2015.<\/a><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>&nbsp;<\/p>\n<table class=\"w7\" frame=\"hsides\" cellspacing=\"0\" cellpadding=\"0\">\n<tbody>\n<tr>\n<td style=\"border: 0px; background-color: #ffffff; text-align: left;\">March\u00a02016<br \/>\nContact: <a href=\"mailto:animal.brc@riken.jp\">Shinya Ayabe, Ph.D.<\/a><br \/>\nExperimental Animal Division, RIKEN BioResource Center<br \/>\nAll materials contained on this site may not be reproduced, distributed, displayed, published or broadcast without the prior permission of the owner of that content.<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>A knock-in mouse strain with R124H human TGFBI mutation B6-Tgfbi&lt;tm1(TGFBI)Ccbko&gt;\u00a0 (RBRC09538) Courtesy of Shigeto Shimmura, M.D., Ph.D. Granular and lattice deposits without edema and neovascul [&hellip;]<\/p>\n","protected":false},"author":19,"featured_media":0,"parent":198,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_seopress_titles_title":"","_seopress_titles_desc":"","_seopress_robots_index":"","_seopress_robots_follow":"","_seopress_robots_imageindex":"","_seopress_robots_snippet":"","_seopress_robots_primary_cat":"","_seopress_robots_breadcrumbs":"","_seopress_robots_freeze_modified_date":"","_seopress_robots_custom_modified_date":"","_seopress_robots_canonical":"","_seopress_social_fb_title":"","_seopress_social_fb_desc":"","_seopress_social_fb_img":"","_seopress_social_fb_img_attachment_id":0,"_seopress_social_fb_img_width":0,"_seopress_social_fb_img_height":0,"_seopress_social_twitter_title":"","_seopress_social_twitter_desc":"","_seopress_social_twitter_img":"","_seopress_social_twitter_img_attachment_id":0,"_seopress_social_twitter_img_width":0,"_seopress_social_twitter_img_height":0,"_seopress_redirections_value":"","_seopress_redirections_enabled":"","_seopress_redirections_enabled_regex":"","_seopress_redirections_logged_status":"","_seopress_redirections_param":"","_seopress_redirections_type":301,"_seopress_analysis_target_kw":"","footnotes":"","_wp_rev_ctl_limit":""},"class_list":["post-13478","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"http:\/\/mus.brc.riken.jp\/ja\/wp-json\/wp\/v2\/pages\/13478","targetHints":{"allow":["GET"]}}],"collection":[{"href":"http:\/\/mus.brc.riken.jp\/ja\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"http:\/\/mus.brc.riken.jp\/ja\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"http:\/\/mus.brc.riken.jp\/ja\/wp-json\/wp\/v2\/users\/19"}],"replies":[{"embeddable":true,"href":"http:\/\/mus.brc.riken.jp\/ja\/wp-json\/wp\/v2\/comments?post=13478"}],"version-history":[{"count":5,"href":"http:\/\/mus.brc.riken.jp\/ja\/wp-json\/wp\/v2\/pages\/13478\/revisions"}],"predecessor-version":[{"id":18599,"href":"http:\/\/mus.brc.riken.jp\/ja\/wp-json\/wp\/v2\/pages\/13478\/revisions\/18599"}],"up":[{"embeddable":true,"href":"http:\/\/mus.brc.riken.jp\/ja\/wp-json\/wp\/v2\/pages\/198"}],"wp:attachment":[{"href":"http:\/\/mus.brc.riken.jp\/ja\/wp-json\/wp\/v2\/media?parent=13478"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}